@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_head {
  this: np:hasAssertion dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_assertion;
    np:hasProvenance dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_provenance;
    np:hasPublicationInfo dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_assertion a np:Assertion .
  
  dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_provenance a np:Provenance .
  
  dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_assertion {
  miriam-gene:10491 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGNe57287c6561a43571b7d3521b87c60c5 sio:SIO_000628 miriam-gene:10491, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_provenance {
  dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_assertion dcterms:description
      "[To explore the possibility that the genetic alterations of CASP, which encodes caspase-6, might be involved in the development of human cancers, we analyzed the entire coding region and all splice sites of the human CASP6 gene for the detection of somatic mutations in 100 colorectal carcinomas and 50 gastric carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:16948818;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP328599.RAPQuNqf_BFDNgOUfzdAw2KW-htnnInCBfs1zhVmLyWdY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:13+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}